HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism.

Abstract
The methyl-binding protein gene, MECP2, is a candidate for involvement in autism through its implication as a major causative factor in Rett syndrome that has similarities to autism. Rare mutations in MECP2 have also been identified in autistic individuals. We have examined the possible broader involvement of MECP2 as a predisposing factor in the disorder. Analysis of polymorphic markers spanning the gene and comprising both microsatellites and single nucleotide polymorphisms (SNPs) by the transmission disequilibrium test in two collections of families (219 in total), one in the USA and one in the UK, has provided evidence for significant association (P = 0.009) for a three-marker SNP haplotype of MECP2 with autism/autism spectrum disorders. This association is supported by association of both Single Sequence Repeat (SSR) and SNP single markers located at the 3' end of the MECP2 locus and flanking sequence, the most significant being that of an indel marker located in intron 2 (P = 0.001 - Bonferroni corrected P = 0.006). This suggests that one or more functional variants of MECP2 existing at significant frequencies in the population may confer increased risk of autism/autism spectrum disorders and warrants further investigation in additional independent samples.
AuthorsC S Loat, S Curran, C M Lewis, J Duvall, D Geschwind, P Bolton, I W Craig
JournalGenes, brain, and behavior (Genes Brain Behav) Vol. 7 Issue 7 Pg. 754-60 (Oct 2008) ISSN: 1601-183X [Electronic] England
PMID19125863 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Genetic Markers
  • MECP2 protein, human
  • Methyl-CpG-Binding Protein 2
  • DNA
  • IRAK1 protein, human
  • Interleukin-1 Receptor-Associated Kinases
Topics
  • Autistic Disorder (epidemiology, genetics)
  • Child
  • DNA (genetics)
  • Genetic Markers
  • Genotype
  • Haplotypes (genetics)
  • Humans
  • Interleukin-1 Receptor-Associated Kinases (genetics)
  • Linkage Disequilibrium (genetics)
  • Methyl-CpG-Binding Protein 2 (genetics)
  • Microsatellite Repeats (genetics)
  • Parents
  • Polymorphism, Genetic (genetics)
  • Polymorphism, Single Nucleotide (genetics)
  • United Kingdom (epidemiology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: